CA1181426A - Hydrocyanation of olefins - Google Patents
Hydrocyanation of olefinsInfo
- Publication number
- CA1181426A CA1181426A CA000412611A CA412611A CA1181426A CA 1181426 A CA1181426 A CA 1181426A CA 000412611 A CA000412611 A CA 000412611A CA 412611 A CA412611 A CA 412611A CA 1181426 A CA1181426 A CA 1181426A
- Authority
- CA
- Canada
- Prior art keywords
- hydrogen cyanide
- effluent
- zone
- catalyst
- temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000005669 hydrocyanation reaction Methods 0.000 title claims abstract description 15
- 150000001336 alkenes Chemical class 0.000 title abstract 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000003054 catalyst Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 6
- 150000002825 nitriles Chemical class 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000011541 reaction mixture Substances 0.000 claims 3
- MXSVLWZRHLXFKH-UHFFFAOYSA-N triphenylborane Chemical compound C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 MXSVLWZRHLXFKH-UHFFFAOYSA-N 0.000 description 7
- BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 description 6
- CFEYBLWMNFZOPB-UHFFFAOYSA-N pent-4-enenitrile Chemical compound C=CCCC#N CFEYBLWMNFZOPB-UHFFFAOYSA-N 0.000 description 5
- 229910018583 Ni(O) Inorganic materials 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- -1 e.g. Chemical group 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- UVKXJAUUKPDDNW-NSCUHMNNSA-N (e)-pent-3-enenitrile Chemical compound C\C=C\CC#N UVKXJAUUKPDDNW-NSCUHMNNSA-N 0.000 description 1
- UVKXJAUUKPDDNW-IHWYPQMZSA-N (z)-pent-3-enenitrile Chemical compound C\C=C/CC#N UVKXJAUUKPDDNW-IHWYPQMZSA-N 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000004799 bromophenyl group Chemical group 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/08—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds
- C07C253/10—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds to compounds containing carbon-to-carbon double bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US307,649 | 1981-10-01 | ||
| US06/307,649 US4382038A (en) | 1981-10-01 | 1981-10-01 | Hydrocyanation of olefins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1181426A true CA1181426A (en) | 1985-01-22 |
Family
ID=23190632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000412611A Expired CA1181426A (en) | 1981-10-01 | 1982-09-30 | Hydrocyanation of olefins |
Country Status (11)
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4990645A (en) * | 1990-06-27 | 1991-02-05 | E. I. Du Pont De Nemours And Company | Hydrocyanation process |
| FR2822820B1 (fr) * | 2001-03-29 | 2003-05-30 | Inst Francais Du Petrole | Procede de coproduction de paraxylene et de metaxylene comprenant deux etapes de separation |
| FR2849027B1 (fr) * | 2002-12-23 | 2005-01-21 | Rhodia Polyamide Intermediates | Procede de synthese de composes comprenant des fonctions nitriles a partir de composes a insaturations ethyleniques |
| FR2850966B1 (fr) * | 2003-02-10 | 2005-03-18 | Rhodia Polyamide Intermediates | Procede de fabrication de composes dinitriles |
| FR2854892B1 (fr) * | 2003-05-12 | 2005-06-24 | Rhodia Polyamide Intermediates | Procede de fabrication de dinitriles |
| FR2854891B1 (fr) | 2003-05-12 | 2006-07-07 | Rhodia Polyamide Intermediates | Procede de preparation de dinitriles |
| DE102004004684A1 (de) * | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Hydrocyanierung |
| WO2007046799A1 (en) * | 2005-10-18 | 2007-04-26 | Invista Technologies S.A R.L. | Process of making 3-aminopentanenitrile |
| WO2007109005A2 (en) * | 2006-03-17 | 2007-09-27 | Invista Technologies S.A R.L. | Method for the purification of triorganophosphites by treatment with a basic additive |
| US7659422B2 (en) * | 2006-07-14 | 2010-02-09 | Invista North America S.A.R.L. | Hydrocyanation process with reduced yield losses |
| US7880028B2 (en) * | 2006-07-14 | 2011-02-01 | Invista North America S.A R.L. | Process for making 3-pentenenitrile by hydrocyanation of butadiene |
| US7919646B2 (en) | 2006-07-14 | 2011-04-05 | Invista North America S.A R.L. | Hydrocyanation of 2-pentenenitrile |
| US7709674B2 (en) * | 2006-07-14 | 2010-05-04 | Invista North America S.A R.L | Hydrocyanation process with reduced yield losses |
| EP2146930A2 (en) | 2007-05-14 | 2010-01-27 | INVISTA Technologies S.à.r.l. | High efficiency reactor and process |
| US8101790B2 (en) * | 2007-06-13 | 2012-01-24 | Invista North America S.A.R.L. | Process for improving adiponitrile quality |
| WO2009091790A1 (en) * | 2008-01-15 | 2009-07-23 | Invista Technologies S.A.R.L. | Hydrocyanation of pentenenitriles |
| CN101910119B (zh) * | 2008-01-15 | 2013-05-29 | 因温斯特技术公司 | 用于制备和精制3-戊烯腈，和用于精制2-甲基-3-丁烯腈的方法 |
| CN101970392A (zh) * | 2008-03-19 | 2011-02-09 | 因温斯特技术公司 | 制备环十二碳三烯的方法和制备月桂内酯的方法 |
| EP2334624B1 (en) * | 2008-10-14 | 2014-10-01 | Invista Technologies S.à.r.l. | Process for making 2-secondary-alkyl-4,5-di-(normal-alkyl)phenols |
| EP2462103A4 (en) * | 2009-08-07 | 2014-01-08 | Invista Tech Sarl | HYDROGENATION AND STAFFING FOR THE FORMATION OF DIES |
| BR112019006983B1 (pt) * | 2016-11-11 | 2023-12-19 | Inventio Ag | Método de operação de um sistema de segurança para edifício e sistema de segurança para edifícios com instalações de elevador |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1112539A (en) * | 1965-11-26 | 1968-05-08 | Du Pont | Preparation of organic nitriles |
| US3496217A (en) * | 1967-05-23 | 1970-02-17 | Du Pont | Hydrocyanation of olefins |
| US3766237A (en) * | 1972-01-25 | 1973-10-16 | Du Pont | Hydrocyanation of olefins |
| US3846461A (en) * | 1972-10-25 | 1974-11-05 | Du Pont | Process of preparing a zerovalent nickel complex with organic phosphorus compounds |
| US3903120A (en) * | 1973-06-19 | 1975-09-02 | Du Pont | Preparation of zerovalent nickel complexes from elemental nickel |
| US4080374A (en) * | 1977-02-23 | 1978-03-21 | E. I. Du Pont De Nemours And Company | Product recovery |
| US4082811A (en) * | 1977-02-23 | 1978-04-04 | E. I. Du Pont De Nemours And Company | Recovery of metal and triarylborane catalyst components from olefin hydrocyanation residue |
| US4328172A (en) * | 1981-02-24 | 1982-05-04 | E. I. Du Pont De Nemours And Company | Hydrocyanation of olefins |
| US4330483A (en) * | 1981-02-24 | 1982-05-18 | E. I. Du Pont De Nemours And Company | Hydrocyanation of olefins |
-
1981
- 1981-10-01 US US06/307,649 patent/US4382038A/en not_active Expired - Lifetime
-
1982
- 1982-09-29 LU LU84393A patent/LU84393A1/fr unknown
- 1982-09-29 NL NL8203771A patent/NL8203771A/nl not_active Application Discontinuation
- 1982-09-30 KR KR8204449A patent/KR880002621B1/ko not_active Expired
- 1982-09-30 GB GB08227990A patent/GB2107314B/en not_active Expired
- 1982-09-30 IT IT23556/82A patent/IT1163012B/it active
- 1982-09-30 FR FR8216446A patent/FR2513995B1/fr not_active Expired
- 1982-09-30 CA CA000412611A patent/CA1181426A/en not_active Expired
- 1982-09-30 JP JP57169926A patent/JPS5867658A/ja active Granted
- 1982-09-30 BE BE0/209125A patent/BE894542A/fr not_active IP Right Cessation
- 1982-10-01 DE DE19823236454 patent/DE3236454A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| KR880002621B1 (ko) | 1988-12-07 |
| DE3236454A1 (de) | 1983-04-21 |
| LU84393A1 (fr) | 1983-06-07 |
| KR840001548A (ko) | 1984-05-07 |
| US4382038A (en) | 1983-05-03 |
| JPS5867658A (ja) | 1983-04-22 |
| IT8223556A0 (it) | 1982-09-30 |
| FR2513995A1 (fr) | 1983-04-08 |
| JPH031298B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-01-10 |
| IT1163012B (it) | 1987-04-08 |
| GB2107314A (en) | 1983-04-27 |
| FR2513995B1 (fr) | 1987-05-07 |
| BE894542A (fr) | 1983-03-30 |
| GB2107314B (en) | 1985-11-20 |
| NL8203771A (nl) | 1983-05-02 |
| DE3236454C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-07-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1181426A (en) | Hydrocyanation of olefins | |
| KR880002296B1 (ko) | 올레핀의 하이드로시안화 방법 | |
| KR950006896B1 (ko) | 할로겐화아연 촉진제를 사용하는 연속 하이드로시안화 반응법 | |
| US4371474A (en) | Hydrocyanation of olefins | |
| KR880002295B1 (ko) | 올레핀의 하이드로시안화 방법 | |
| US4874884A (en) | Promoter synergism in pentenenitrile hydrocyanation | |
| CA2214009C (en) | Process for hydrocyanation in the presence of zero-valent nickel, a bidentate phosphorous compound and a lewis acid | |
| US4387056A (en) | Process for separating zero-valent nickel species from divalent nickel species | |
| JP4509124B2 (ja) | １，３−ブタジエンのヒドロシアン化によるアジポニトリルの製造 | |
| US8410299B2 (en) | Method for producing linear pentenenitrile | |
| EP2041075B1 (en) | Process for making 3-pentenenitrile by hydrocyanation of butadiene | |
| US3564040A (en) | Removal of trans-2-pentenenitrile from 3- and 4-pentenenitrile | |
| KR101064039B1 (ko) | 3-펜텐니트릴의 제조방법 | |
| EP2041074B1 (en) | Hydrocyanation of 2-pentenenitrile | |
| EP0160296B1 (en) | Recovery of zerovalent nickel complexes | |
| JP2694215B2 (ja) | アジポニトリルの製造方法 | |
| EP1344770A1 (en) | Process for the hydrocyanation of butadiene | |
| US3652641A (en) | Hydrocyanation of olefins |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEC | Expiry (correction) | ||
| MKEX | Expiry |